Today, on the seven month anniversary of my daughter's diagnosis, we booked a cruise. We haven't really traveled much since her diagnosis, and we're still relatively new to this whole nightmare, so I was wondering what tips anyone else has for traveling with a T1 kid. I'm a little anxious about being away from a pharmacy, but our CDE just told me to figure out what I thought that I would need and pack triple. There are medical providers on the ship, (and my ex is traveling with us--he's a kidney specialist), so I think taht we will be well supported. But the logistics of all of this are pretty daunting. would love to hear from more experienced people....
I've never been on a cruise so I don't know what to expect. =) I do always pack double (back up meter too) but I think if I went on a cruise I would pack triple. I always have a letter of nessesity in case supplies are questioned but they never have been. Maybe you can check about getting a fridge in your room? A mom I met bought a tiny little fridge to bring on a cruise with her to keep her sons insulin in. Thought that was interesting. =)
We took a road trip to FL not long after my son was Diagnosed. As long as you take extra supplies and make sure to keep your schedule you will be ok :)
On a side note I think you should take me with you just to be safe (giggles)
I have bought a few medical storage bags for trips but I was never really happy with them. I found a large cosmetic travel case, probably the size of a large binder that opens like a book with clear pockets on each side. It worked great and was easy to put in my carry on and if security needed to look at it then I could just open the main zipper and they could see everything.
I always carry crystal light packs and fruit chews with me, too. My husband used to make fun of me because I would pack Crystal light in our suitcases. They have come in so handy at places like Disney World.
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- Heatherkansas
on Feb. 6, 2012 at 10:42 PM